N-isopropyl-phosphoro-amido-thioates

ABSTRACT

N-ISOPROPYL-PHOSPHORO-AMIDO-THIOATES, I.E. O-(2NITRO-4-ALKOXY-PHENYL)-O-ALKYL-N-ISOPROPYL-PHOSPHORO-AMIDO-THIOATES OR O-(2-NITRO-4-ALKOXY-PHENYL)O-ALKYL-N-IDOPTOPYL-SMIFO-YHIONOPHODPHSYRD, EHIVH POSSESS HERBICIDAL PROPERTIES AND WHICH MAY BE PRODUCED BY CONVENTIONAL METHODS.

United States Patent US. Cl. 260-951 Claims ABSTRACT OF THE DISCLOSURE N-isopropyl-phosphoro amido thioates, i.e. O (2- nitro 4 al'koxy phenyl) O alkyl-N-isopropyl-phosphoro-amido-thioates or O (2 nitro 4-alkoxy-phenyl)- O alkyl N isopropyl amido-thionophosphates, which possess herbicidal properties and which may be produced by conventional methods.

The present invention relates to and has for its objects the provision for particular new N-isopropyl-phosphoroamido-thioates, i.e. O (2 nitro 4 alkoxy phenyl)- O alkyl N isopropyl phosphoro amido thioates or 0-(2 nitro 4 alkoxy phenyl) O alkyl-N-isopropylamido-thionophosphates, which possess herbicidal properties, active compositions in the form of mixtures of such compounds with solid and liquid dispersible carrier vehicles, and methods for producing such compounds and for using such compounds in a new way, especially for combating weeds, undesired plants, and the like, with other and further objects becoming apparent from a study of the within specification and accompanying examples.

It is already known that pentachloro-phenol (A), commonly known as PCP, and 2,4-dichloro phenyl-4'-nitrophenyl-ether (B), commonly known as NIP, as well as 2 chloro 4,6 bis(ethy1amino) 1,3,5 triazine (C), commonly known as CAT or Simazin, posses herbicidal properties.

It is furthermore known from British Patent 659,682

that amido-thionophosphoric acid esters of the formula X m R1 I -OX in which R is an alkyl or alkenyl radical, R is an alkyl radical, R is an alkyl radical or a hydrogen atom, and one X is a nitro radical and the other X is a hydrogen atom or a nitro radical, possess insecticidal and fungicidal properties. In said British Patent, it is indicated only that such compounds have insecticidal and acaricidal activity as well as activity for the control of harmful fungi on plants, and that they can be used in the form of spray preparations. However, there is no actual test data showing their eflicacy, and no indication that such compounds might have herbicidal activity. Furthermore, no mention is made of the applicability of such compounds to soil or of any reason to expect them to have herbicidal activity.

On the other hand, US. Pat. 3,074,790 describes compounds, for example 0 (2,4 dichloro phenyD-O- methyl N -isopropy1 phosphoro amido thioate (D), which have herbicidal properties.

In accordance with Japanese PatentApplication No. 78,104/66 (filed on Nov. 30, 1966), i.e. corresponding to U.S. 3,472,920, dated Oct. 14, 1969, it has been found 3,705,929 Patented Dec. 12, 1972 that a certain derivative of this last-mentioned type of amido thiono phosphoric acid ester (which may be prepared in the same manner as the compounds of the present invention) as especially excellent herbicidal activity, to wit, O-(Z-nitro-phenyl)-O-methyl-N-isopropylphosphoro-amido-thioate of the formula:

N01 CHaO S It has now been found, in accordance with the present invention, that the particular new N isopropyl phosphoro amido thioates, i.e. O (2 nitro 4 alkoxyphenyl) 0 alkyl N isopropyl-phosphoro-amidothioates, of the formula in which R is alkyl of 1-4 carbon atoms, and R is alkyl of 1-4 carbon atoms,

ROS

l-CaH1N (II) in which R is the same as defined above, and

Hal is a halogen atom such as chloro, bromo, iodo or fiuoro, especially chloro,

with a 2-nitro-4-alkoxy-phenol of the formula in which R is the same as defined above, and

M is hydrogen, or a cation such as an ammonium or alkali metal cation, for example potassium, sodium, and the like;

(III) (b) Reacting an N-isopropyl-amido-thionophosphoric acid dihalide of the formula Hal in which Hal is the same as defined above,

either with a 2-nitro-4-alkoxy-phenol of Formula III and then with an alcoholate of the formula:

in which R is the same as defined above, and

M is a cation such as an alkali metal cation, for example potassium, sodium, and the like,

or with the alcoholate of Formula V, and then with the 2-nitro-4-alkoxy-phenol of Formula III.

Surprisingly, the particular new compounds according butyl)-N-isopropyl-amidothionophosphoric acid ester to the present invention show both a higher and more chlorides, bromides, iodides and fluorides. specific herbicidal elfectiveness than the previously known As examples of N-isopropyl-amido-thionophosphoric compounds which are known to be usable for such puracid dihalides of Formula IV above which may be used as poses, e.g. compounds (A), (B) and (C) above. The 5 starting materials, there are mentioned: the correspondinstant compounds are especially elfective as preemergence ing di-chlorides, bromides, iodides and fluorides. herbicides, and exhibit a remarkable effect in killing weeds, As examples of 2-nitro-4-alkoxy-phenols of Formula with only slight, if any, phytotoxic efiect toward cultivated III above which may be used as starting materials, there plants such as rice. The instant compounds therefore are mentioned: 2-nitro-4-(methoxy, ethoxy, nand isorepresent a valuable contribution to the art. P P Y and ten-'butoxw'phenolsi and the Advantagemlsly, in accordance with the Present corresponding ammonium, potassium and sodium salts vention, in the various formulae herein: h f,

R represents straight and branched chain lower alkyl As examples of alcoholates of Formula V above which hydrocarbon 0f carbon atoms Such as y y may be used as starting materials, there are mentioned: 11- and iso-propyl, n-, iso-, sec.- and tert.-butyl, and the 15 potassium and sodium methylate, ethylate, nand isolike, especially C or C alkyl; and propylate, and n-, iso-, sec.- and tert.butylate.

R represents straight and branched chain lower alkyl By means of reaction variant (a), the active compounds hydrocarbon of 1-4 carbon atoms such as methylto of the present invention can be prepared easily and in text-butyl inclusive as defined above, and the like, especimarkedly good yields.

ally C or methyl; Process variant (2.) is preferably carried out in the R and R being the same or diflerent. presence of an inert organic solvent (this term includes The reaction course according to process variant (a) is a mere diluent). Examples of such solvents include illustrated by the following formula scheme: aliphatic or aromatic hydrocarbons (which may be halo- NO: R0 8 N0: \ll RO\fi /PO OR MHal P-Hal M o- R 1-O=H1NH i-CaHiNH The starting materials which may be used for reaction genated), for example benzine, methylene chloride, chlovariant (a) are clearly characterized by Formulae H and roform, carbon tetrachloride, benzene, chlorobenzene,

III above, and are well known. toluene, and xylene; ethers, for example diethyl ether,

The reaction course according to process variant (b) is dibutyl ether, dioxan, and tetrahydrofuran; aliphatic illustrated by the following formula scheme: alcohols or ketones which have low boiling points, for

NO: R0 8 I N0: \H Eek? /P0 OR' M nn P-O R M G-R i-GaHzNH IH7NH (III') The reaction course of the alternative of variant (b) is example methanol, ethanol, isopropanol, acetone, methyl illustrated by the following formula scheme: ethyl ketone, methyl isopropyl ketone, and methyl iso- R0 8 \II si/Hal P-Hal MHal i-caH-lNH-l il- M"GR -r l-CIH'INH Hal No: R0 8 N01 RO\'S P-O OR MHai l -Hal M 0 R l-C H1NH l-CzH7NH The starting materials which may be used for reaction butyl ketone; and the like. Lower aliphatic nitriles, for variant (b) and the alternative of reaction variant (b) are example acetonitrile, propionitrile, and the like, may also clearly characterized by Formulae III, IV and V above, be used.

and are well known. If M is hydrogen in the appropriate starting compound As examples of O-alkyl-N-isopropyl-amido-thiono-phosof Formula III above, the reaction according to variant phoric acid ester halides of Formula II above which may (a) may preferably be carried out in the presence of an be used as starting materials, there are mentioned: 0- acid-binding agent. Examples of these include alkali metal (methyl, ethyl, nand iso-propyl, n-, iso-, sec.- and tcrt. carbonates and bicarbonates or alcoholates, such as potassium carbonate, sodium bicarbonate, sodium carbonate, or sodium or potassium methylate or ethylate, or aliphatic, aromatic or heterocyclic tertiary bases such as triethylamine, diethylaniline, pyridine, and the like. Instead of using an acid-binding agent, a salt of the 2-nitro-4-alko-xyphenol of Formula III above may be prepared, preferably an alkali metal or ammonium salt, and then this salt may be reacted with the starting O-alkyl-N-isopropyl-amidothiono-phosphoric acid ester halide of Formula II above.

The reaction according to process variant (:1) may be carried out within a fairly wide temperature range, but in general at temperatures from substantially between about -l10 0, preferably between about -70 C.

In carrying out process variant (b) one may for example proceed as follows:

1 mol of alkali metal or ammonium salt of 2-nitro-4- alkoxy-phenol of Formula III above is dissolved in one of the above-noted solvents, preferably alcohol, and the solution is added dropwise to 1 mol of N-isopropyl-amdiothionophosphoric acid dihalide of Formula IV above and the mixture is heated at 70 C. for a short time. Then the mixture is cooled to room temperature and mixed with 1 mol of alcoholic solution of alkali metal alcoholate. For completing the reaction, the reaction mixture is again heated at 4070 C. for a short time and excess alcohol is distilled off under reduced pressure. The residue is dissolved in a Water-immiscible solvent, preferably one of the aforementioned hydrocarbons or ethers, and the solution is washed with water. After washing with a solution of dilute alkali metal hydroxide or ammonium hydroxide, the organic phase is dried and finally, by removing the solvent by distillation, the desired compound is obtained as the residue.

Alternatively, the sequence of adding the starting materials for process variant (b) may be reversed. In this case, the N-isopropyl-amido-thionophosphoric acid dihalide of Formula IV above is reacted at first with, e.g. an alkali metal alcoholate, solution of an alcoholate of Formula V above, and then the intermediate product formed is reacted with the 2-nitro-4-alkoxy-phenol of Formula III above. When applying this alternative, the conditions of the reaction may be the same as those mentioned above.

Advantageously, the instant active compounds exhibit a strong herbicidal potency and can therefore be used as germination inhibiting agents or weed-killers. By weeds in the sense used herein are meant all plants which grow in places where they are not desired. Whether the active compounds according to the present invention act as total or selective herbicidal agents depends on the amount applied, as the artisan will appreciate.

The active compounds according to the present invention can be used for example in the case of the following plants: dicotyledons, such as mustard (Sinapis), cress (Lepidium), catch weed (Galium), common chickweed (Stellaria), camomile (Matricaria), French weed (Galinsoga), goose-foot (Chenopodium), stinging nettle (Urtica), groundsel (Senecio), wild amaranth (Amaranthus), common purslane (Portulaca), cotton (Gossypium), beets (Beta), carrots (Daucus), beans (Phaseolus), potatoes (Solanum), coffee (Coifea), cabbage (Brassica), spinach (Spinacia); monocotyledons, such as timothy (Phleum), meadowgrass (Poa), fescue (Festuca), finger grass (Digitaria), goosegrass (Eleusine), green foxtail (Setaria), raygrass (Lotium), cheat (Bromus), barnyard grass (Echinochloa), maize (Zea), rice (Oryza), oats (Avena), barley (Hordeum), wheat (Triticum), millet (Panicum) and sugar cane (Saccharum); and the like.

The instant compounds are preferably used as selective herbicides and especially when applied to soil before germination, although they exhibit a particularly good selectivity when applied before and after emergence, e.g. in upland and paddy fields where cucumber, tomato, cotton, sugar beets, carrots, beans, potatoes, coffee, cab- 6 bage, spinach, raddish, maize, rice, oats, barley, wheat, millet and sugar cane are cultivated.

Signficantly, the active compounds of the present invention are distinguished by the fact that they are not phytotoxic to rice plants although they are markedly effective in small dosages as compared with PCP and NIP, i.e. compounds (A) and (B), etc. which have hitherto been used widely as herbicides in paddy fields. Furthermore, the same effect as with CAT or Simazin, i.e. compound (C), is generally achievable using the instant active compounds without any harm to crops when applied to soil before germination for controlling weeds in upland fields. Especially when applied to soil before germination, the instant compounds are far better than the already known herbicides in that such instant compounds show a superior selective henbicidal activity, depending on the amount applied.

The active compounds according to the present invention significantly also show a secondary insecticidal and fungicidal activity, e.g. against insects and phytopathogenic fungi which infest plants.

The active compounds according to the instant invention can be utilized, if desired, in the form of the usual formulations or compositions with conventional inert (i.e. plant compatible or herbicidally inert) pesticidal diluents or extenders, i.e. diluents or extenders of the type usable in conventional pesticidal formulations or compositions, e.g. conventional pesticidal dispersible car rier vehicles, such as solutions, emulsions, suspensions, emulsifiable concentrates, spray powders, pastes, soluble powders, dusting agents, granules, etc. These are prepared in known manner, for instance by extending the active compounds with conventional pesticidal dispersible liquid diluent carriers and/or dispersible solid carriers optionally with the use of carrier vehicle assistants, e.g. conventional pesticidal surface-active agents, including emulsifying agents and/ or dispersing agents, whereby, for example, in the case where Water is used as diluent, organic solvents may be added as auxiliary solvents. The following may be chiefly considered for use as conventional carrier vehicles for this purpose: inert dispersible liquid diluent carriers including inert organic solvents, such as aromatic hydrocarbons (e.g. benzene, toluene, xylene, etc.), halogenated, especially chlorinated, aromatic hydrocarbons (e.g. chloro-benzenes), paraffins (e.g. petroleum fractions), chlorinated aliphatic hydrocarbons (e.g. methylene chloride, etc.), alcohols (e.g. methanol, ethanol, propanol, butanol, etc.), ethers, etheralcohols (e.g. glycol monomethyl ether, etc.) amines (e.g. ethanolamine, etc.), amides (e.g. dimethyl formamide, etc.), sulfoxides (e.g. dimethyl sulfoxide, etc.), ketones (e.g. acetone, etc.), and/or water; as well as inert dispersible finely divided solid carriers, such as ground natural minerals (e.g. kaolins, alumina, silica, chalk, i.e. calcium carbonate, talc, kieselguhr, montmorillonite, clay, etc.), and ground synthetic minerals (e.g. highly dispersed silicic acid, silicates, e.g. alkali silicates, etc.); whereas the following may be chiefly considered for use as conventional carrier vehicle assistants, e.g. surface-active agents, for this purpose: emulsifying agents, such as nonionic and/or anionic emulsifying agents (e.g. polyethylene oxide esters of fatty acids, polyethylene oxide ethers of fatty alcohols, alkyl sulfonates, aryl sulfonates, etc., and especially alkyl aryl-polyglycol ethers, magnesium stearate, sodium oleate, etc.); and/or dispersing agents, such as lignin, sulfite waste liquors, methyl cellulose, etc.

As will be appreciated by the artisan, the active compounds according to the instant invention may be employed alone or in the form of mixtures with one another and/or with such solid and/or liquid dispersible carrier vehicles and/or with other known compatible active agents, especially plant protection agents, such as other herbicides, or fungicides, insecticides, acaricides, nematocides, bactericides, plant growth regulators, soil disinfectants, etc., including phenoxy compounds, chlorophenol compounds, carbamates, diphenyl ethers, and triazine compounds, and other known agricultural chemicals and/or fertilizers, etc., if desired, or in the form of particular dosage preparations for specific application made therefrom, such as solutions, emulsions, suspensions, powders, pastes, and granules which are thus ready for use.

As concerns commercially marketed preparations, these generally contemplate carrier composition mixtures in which the active compound is present in an amount substantially between about 0.1 and 95% by weight, and preferably 0.5 and 90% by weight, of the mixture, Whereas carrier composition mixtures suitable for direct application or field application generally contemplate those in which the active compound is present in an amount substantially between about 0.00510%, preferably 0.008- by weight of the mixture. Thus, the present invention contemplates over-all compositions which comprise mixtures of a conventional dispersible carrier vehicle such as (l) a dispersi-ble inert finely divided carrier solid, and/or (2) a dispersible carrier liquid such as an inert organic solvent and/ or water preferably including a surface-active effective amount of a carrier vehicle assistant, e.g. a surface-active agent, such as an emulsifying agent and/or a dispersing agent, and an amount of the active compound which is effective for the purpose in question and which in generally between about ODDS-95%, and preferably 0.008-95%, by weight of the mixture.

In particular, the amount of active compound applied per imit area varies according to the purpose intended, i.e. the effect desired, and the mode of application. In general, higher quantities of substantially between about 5- 40 kg. of active compounds per hectare are applied for total or non-selective herbicidal activity, whereas lower quantities of substantially between about 1.25-5 kg. of active compound per hectare are applied for selective herbicidal activity, these amounts per unit area being irrespective of whether or not a carrier vehicle is also present.

The active compounds can also be used in accordance with the well-known ultra-low-volume process with good success, i.e. by applying such compound if normally a liquid, or by applying a liquid composition containing the same, via very effective atomizing equipment, in finely divided form, e.g. average particle diameter of from 50-100 microns, or even less, i.e. mist form, for example by airplane crop spraying techniques. Only up to at most about a few liters/hectare are needed, and often amounts only up to about 1 quart/acre, preferably 2-16 fluid ounces/acre, are suilicient. In this process it is possible to use highly concentrated liquid compositions with said liquid carrier vehicles containing from about 20 to about 95% by weight of the active compound or even the 100% active substance alone, e.g. about 20- 100% by weight of the active compounds.

While the active compounds can be used particularly effectively according to the pre-emergence method, they are also effective when used according to the post-emergence method.

Especially when application is carried out mainly before the germination of cultivated plants, the general onditions of cultivation are not so important, but the quantity of active compound to be applied per unit area and the application method are important, as the artisan will appreciate.

Furthermore, the present invention contemplates methods of selectively killing, combating or controlling undesired plants, e.g. weeds and the like, which comprise applying to at least one of (a) such weeds and (b) their habitat, i.e. the locus to be protected, a herbicidally effective or toxic, amount of the particular compound of the invention alone or together with a carrier vehicle as noted above. The instant formulations or compositions are ap- 8 plied in the usual manner, for example by spraying, atomizing, scattering, dusting, watering, sprinkling, and the like, whether for pre-emergence application to the soil or post-emergence application to the weeds.

It will be realized, of course, that in connection with the pre-emergence use of the instant compounds as well as the post-emergence use thereof, the concentration of the particular active compound utilized in admixture with the carrier vehicle, and the amounts applied per unit area, will depend upon the intended application and may be varied within a fairly wide range depending upon the weather conditions, the soil, the purpose for which the active compound is used, e.g. for total or only selective herbicidal effect, and the plants which are to be controlled or protected. Therefore, in special cases, it is possible to go above or below the aforementioned concentration ranges and amounts per unit area.

The following illustrate, without limitation, examples of formulations which may be used in accordance with the present invention:

FORMULATION A 5% by weight of instant compound (1), and by weight of a mixture of talc and clay (3:1) are formulated into a dust by mixing and crushing. It is applied as is by dusting to weed and/or their habitat.

FORMULATION B- 20% by weight of instant compound (4), 75% by weight of a mixture of talc and clay (3:1), 3% by weight of sodium alkylbenzene sulfonate, and 2% by weight of sodium dinaphthylmethane disulfonate are formulated into a wettable powder by mixing and crushing. It is diluted with water at the concentration of 1 to 500, and applied by spraying to weeds and/or their habitat.

FORMULATION C 20% by weight of instant compound (4), 75% by weight of xylol, and 5% by weight of emulsifier Sorpol (trade name of the product of Toho Kagaku Kogyo K.K., Japan: polyoxyethylenealkylarylether) are formulated into an emulsifiable concentrate by mixing and stirring. It is diluted with water at the concentration of 1 to 1,000 and applied by spraying to weeds and/or their habitat.

FORMULATION D Instant compound (5) is dissolved in xylol, and the solution is sprayed onto clay granules while rotating and mixing so that about 10% by weight of the active compound is contained thereon. The granular formulation is applied by scattering on the surface of soil.

The herbicidal effectiveness of the particular new compounds of the present invention is illustrated, without limitation, by the following examples:

Example 1.-Test against weeds of paddy fields Preparation of active compounds:

Carrier vehicle-5 parts by weight of acetone or 5 parts by weight of talc Emulsifier-l part by weight of benzyloxypolyglycolether To produce a suitable preparation of the particular active compound, 1 part by weight of such active compound is mixed with the stated amount of carrier vehicle and the stated amount of emulsifier intimately, and the resulting emulsifiable concentrate or wettable powder is then diluted with water to the desired final concentration.

Test method: Pots of a. are charged with paddy field soil and then filled with water. Paddy rice seedlings (Kinmaze variety) of 3 to 4 leaves stage are transplanted into the pots under irrigated conditions. After the seedlings have taken root, seeds of barnyardgrass and broad-leaved weeds are sown and spikerush are planted in such pots simultaneously.

The preparations of the given active compound are sprayed at the rate of 500, 250 and 125 g. of active compound per 10 a. onto the soil of the pots. After 3 weeks, the degree of damage against the barnyardgrass, spikerush and broad-leaved weeds and the phytotoxicity to the paddy rice are determined and characterized by the values to 5, which have the following scales:

Herbicidal eflicacy: Phytotoxicity -Plants are completely dead or no germination occurs 5&p1z1ints are completely ea 4-Plants are partially destroyed or 20% or less germinated 4-remarkable damage. 3-P 1 a n t s are remarkably damaged or 50% or less germinated 2Plants are markedly damaged or 70% or less germinated 1-Plants are slightly damaged or 90% or less germinated 1-slight damage. 0No effect -0-no phytotoxicity.

3marked damage.

2small damage.

The particular active compounds tested and the results obtained can be seen from the following Table 1:

TABLE 1.HERBICIDAL EFFECT AGAINST WEEDS OF PADDY FIELDS AND PHYIOTOXICITY TO RICE Herbicidal effect Phyto- Amount toxicity of active Barn- Broad- Active compound yard Spikeleaved Paddy Compound No. in, g./ a. grass rush weeds rice Compounds of invention:

(71) 500 5 5 5 0 250 4 4 5 0 125 4 3 4 0 Known compoundscomparison:

(A) pentachloro phenol 500 5 3 5 0 250 3 0 2 0 125 1 0 0 0 TABLE 1Continued NOTES. (1) Broad-leaved weeds are Monochoria Rotala indicu, K oelme, Lmderrtia pyxidaria, Gratiola japom'ca Miguel etc. (2) Compounds 0! 1I1V8Ill2l0l1 have corresponding numbers to those in Table 4 below.

Example 2.Test against weeds of upland fields Preparation of active compounds:

Carrier vehicle-5 parts by weight of acetone or 5 parts by weight of talc Emulsifier1 part by weight of benzyloxypolyglycolether To produce a suitable preparation of the particular active compound, 1 part by weight of such active compound is mixed with the stated amount of carrier vehicle and the stated amount of emulsifier intimately, and the resulting emulsifiable concentrate or wettable powder is then diluted with water to the desired final concentration.

Test method: Pots of 30 x 30 cm. are charged with soil of diluvial volcanic ash. Seeds of the below-mentioned weeds, upland rice (Hataminori variety) and vegetables are sown, and then the preparations of the given active compound are sprayed at the rate of 400, 200 and 100 g. of active compound per 10 a. on the surface of the soil of the pots. After 3 weeks, the herbicidal effect against various kinds of weeds and the phytotoxicity to upland rice and certain vegetables are determined and character ized by the values 0 to 5, which have the following scales:

Herbicidal eflicacy: Phytotoxicity 5-plants are completely dead or no germination occurs 5plants are completely dead or no germination occurs. 4-plants are partially destroyed after germination or 20% or less germinated 4plants are remarkably damaged after germination or 50% or less germinated. 3-plants are remarkably damaged after germination or 50% or less germinated 3plants are markedly damaged after germination or 70% or less germinated. 2plants are markedly damaged after germination or 70% or less geri d 2plants are considerably damaged after germination or 70% or more germinated.

1plants are slightly damaged after germination or or less germinated 1-plants are slightly damaged after germination or 90% or more germinated. 0-no etfect 0no phytotoxicity.

The particular active compounds tested and the results obtained can be seen from the following Table 2.

TABLE 2.-HE RBICIDAL EFFECT AGAINST WEEDS OF UPLAND FIELDS AN D PHYTOIOXIGITY TO VARIOUS CROPS Herbieldal effect of- Wild Barnamar- Phytotoxleity of- Amonnt yard- Finger- Dent anth Common of active grass grass ioxtail (Amapurslane Japeompound, (Eehino- (Digl- (Sotran- (Portu- Upland anese Cueum Car- .Aotive Compound No. g./10 a. chloa) taria) aria) thus) lac rice radish ber Tomato rot;

Compounds of invention:

(72) ...t 400 5 5 5' 5 5 o o o 0 0 200 5 5 4 5 5 0 0 0 O 0 100 5 4 4 5 4 0 0 0 0 0 Known compoundseomparison:

(C) 2-ehloro-4,6-bis (ethylamine) -1, 3, 5-trlazine 100 5 5 5 5 5 2 3 2 2 2 (B) 2, 4-diehloro-phenyl-4'- nitrophenyl ether 400 5 5 5 5 5 3 1 5 5 5 200 5 5 4 5 5 0 0 2 2 3 Control 0 0 0 0 0 0 D 0 0 0 N OTB-Compounds of invention have corresponding numbers to those in Table 4 below.

Example 3.-Test of pro-emergence soil treatment against various plants To produce a suitable preparation of the particular active compound, 1 part by weight of such active compound is mixed with 5 parts by weight of solvent (acetone) and 1 part by weight of emulsifier (benzyloxypolyglycol ether), and the resulting emulsifiable concentrate is then diluted with water to the desired final concentration.

Seeds of the test plants are sown in normal soil and after 24 hours the preparation of the given active compound is sprayed onto the test plants. After 3 Weeks, the

characterized by the values 0 to 5, which have the following meaning:

The particular active compounds tested, their amount per unit area, and the results obtained can be seen from degree of damage to the test plants is determined and the following Table 3:

TABLE 3.-PREEMERGENCE SOIL TREATMENT AGAINST VARIOUS PLANTS (POT TEST) Amount of active compound Amain Cot- Cab- Eelnno- Portu- Cheno- Stelran- Digi- Aetive Compound No. kgJha. Wheat Barley Rice ton Maize bago ehloa laoa podium lan'a thus taria Known oompounds comparison:

(D) O-(2,4-diohlorophenyl)- 20 2-3 2-3 3 2 3 2-3 5 5 5 5 4 5 O-rnethyl-N-isopropyl- 10 1 1 1 1 2 1 5 4 5 5 3 5 phosphoroamidothioate. 5 0 0 0 0 0 0 5 2 5 3 1 5 (E) O-(Q-nitrophenyD-G- 2O 4 4 5 4 3 4-5 5 5 5 5 5 5 methyl-N-isopropyl- 10 1-2 2 3 2 2 2 5 5 5 5 5 5 phosphoroamidothioate. 5 o 0 0 0 0 0 5 5 5 5 4-5 5 Compounds of invention:

N on: .--Con1pounds of invention have corresponding numbers to those in Table 4 below.

The test results described in the above-mentioned Table 3 show that the compounds of the present invention have excellent selective herbicidal efiect without causing any phytotoxicity to cultivated plants when used in a suitable quantity (e.g. 1.25 kg.-5 kg. of active compound per hectare). Especially excellent herbicidal etfect is shown against barnyardgrass (Echinochloa), fingergrass (Digitaria), common purslane (Portulaca), wild amaranth (Amaranthus), etc.

The following further examples illustrate, without limitation, the process for producing the particular new compounds of the present invention.

Example 4 [reaction variant (a)] 17.0 g. (0.1 mol) of 2-nitro-4-methoxy-phenol are dissolved in 100 m1. of acetonitrile, and 14.0 g. of potassium carbonate are added to the resulting solution. 20 g. (0.1 mol) of O ethyl-N-isopropyl-amido-thionophosphoric acid ester chloride are added dropwise at 50-60 C. with vigorous stirring. The mixture is heated and further stirred at 70 C. for 5 hours to complete the reaction. The inorganic salt produced is filtered off and the filtrate is distilled to remove the solvent. The residue is dissolved in 100 ml. of benzene. The benzene solution is washed with 1% solution of sodium carbonate, dried over anhydrous sodium sulfate and distilled off. The crude product is extracted with a carbon tetrachloride/n-hexane mixture. By distilling oil the solvent, 25 g. of O-(2-nitro-4-methoxyphenyl) ethyl-N-isopropyl-phosphoro-amido-thioate, 11 1.5370, are obtained.

In an analogous manner, O-(2-nitro-4-ethoxy-phenyl)- O-ethyl-N-iso-propyl-phosphoro-amido-thioate and 14 O (2-nitr0-4-isopropoxy-phenyl) -O-ethyl-N-isopropylphosphoro-amidothioate (8 are obtained when 2-nitro-4- eth'oxy-phenol or 2-nitro-4-isopropoxy-pheuol are used, respectively, instead of 2-nitro-4-methoxy-phenol. These compounds also have similar herbicidal activity to the aforementioned compound.

Example 5 [reaction variant (a)] N02 CHaO S LO mm 84 g. (0.5 mol) of 2-nitro-4-methoxy-phenol are dissolved in 400 ml. of acetonitrile, and g. of dried and sifted potassium carbonate are added to the resulting solution. g. (0.5 mol) of O-methyl-N-isopropyl-amido-thionophosphoric acid ester chloride are added dropwise at 50-60 C., with vigorous stirring. The mixture is heated at 60 C. for 5 hours to complete the reaction. The inorganic salt produced is filtered off and the filtrate is distilled to remove the solvent. The residue is dissolved in ml. of benzene. The benzene solution is washed with a 1% aqueous solution of sodium carbonate and dried over anhydrous sodium sulfate. After distilling off the benzene and recrystallizing the residue from a carbon tetrachloride/n-hexane mixture, g. of O-(2-nitro-4-me thoxy phenyl)-O-methyl-N-isopropyl-phosphoro-amidothioate, M.P. 69'-70 C., are obtained.

In an analogous manner, O-(2-nitro-4-methoxy-phenyl)- O isopropyl-N-isopropyl-phosphoro-amido-thioate, n 1.5369, (6 having similar herbicidal activity, is obtained when the corresponding O-isopropyl-N-isopropyl-amido- -thiono-phosphoric acid ester chloride is used instead of O-methyl-N-isopropyl-amido-thionophosphoric acid ester chloride.

The following Table 4 illustrates appropriate data for typical compounds of the present invention.

TABLE 4 Compound Structural formula Chemical name (15) H O S 702 0'(2-nltr0-4-meth0 yp enyl)-O-Inethyl-N-lsopropyl-phosphoroamido-thloate.

P-O 0 OH: i-Ca 1 (2.) N01 0-(2-nitro-4-ethoxypl1enyl)-O-methyl-N-isopropyl-phosphoroamldo-thioate.

CHaO fi P-O- 0 (32H.

l-Ca 1 (3 H O S N 02 0-(Z-nitro-4-n-prop0xyphenyl)-O-methyl-N-isopropyl-phosphoroamldo-thioate.

P-O- O C m-n l-Ca 1 (4 NO: O-(2-nltro4-methoxyphenyl)-O-ethyl-N-tsopropyl-phosphoroamido-thloate.

P-O- O CH:

i-ca r (5 H N01 O-(2-nitr0-4-eth0xyphenyl)-0-ethyl-N-isopropyl-phosphoroamldo-thioate.

C1 50 S H o o 0.... l-C aH' Nfi (6 0 N01 0-(2-nltro-4methoxyphenyl)-O isopropyl-N-isopropyl-phosphoroamido-thioate.

1-CaH1 S ll /PO O CH: l-OaH1NH (7 N 0.! 0-(2-nltro4-methoxyphenyl)-0-n-buty1-N-lsopropyl-phosphoroamido-thloate.

Il-C Hn0 S /P-O O 0 H3 H3 a 7N (8,) 0 S N01 0-(2-nltro-4lsopropoxyphenyl)-O-ethyl-N-isopropyl-phosphoroamido-thloate.

P-O-QO 0 3111-1 :It will be realized by the artisan that all of the foregoing compounds contemplated by the present invention possess the desired selective or total herbicidal properties, and especially the capability of selectively destroying Weeds, as well as a comparatively low toxicity toward warm-blooded creatures and a concomitantly low phytotoxicity with respect to higher plants, enabling such compounds to be used with correspondingly favorable compatibility with respect to warm-blooded creatures and higher plants for more effective control and/or elimination of weeds by selective application of such compounds to such weeds and/or their habitat. Nevertheless, the instant compounds posses total herbicidal action when used in large quantities, although selective herbicidal action is obtained when used in smaller quantities. As contemplated herein, the term weeds" is meant to include not only weeds in the narrow sense, but also in the broad sense, whereby to cover all plants and vegetation considered undesirable for the particular purposes in question.

It will be appreciated that the instant specification and examples are set forth by way of illustration and not limitation, and that various modifications and changes may be made without departing from the spirit and scope of the present invention.

What is claimed is:

1. N-isopropyl-phosphoro-amido-thioate of the formu' la in which R is alkyl of 1-4 carbon atoms and R is alkyl of 1-4 carbon atoms.

2. Compound according to claim 1 wherein R is alkyl of from one to three carbon atoms.

3. Compound according to claim 1 wherein R is alkyl of from one to three carbon atoms and R is methyl.

4. Compound according to claim 1 wherein such compound is O-(2-nitro-4-methoxy-phenyl)-O-methyl-N-isopropyl-phosphoro-amido-thioate of the formula orno s i-oQ-o CH:

5. Compound according to claim 1 where in such compound is O (Z-nitro-4-methoxy-phenyl)-O-ethyl-N-isopropyl-phosphoro-amido-thioate of the formula 6. Compound according to claim 1 wherein such compound is O (2-nitro-4-methoxy-phenyl)-O-isopropyl-N- isopropyl-phosphoro-amido-thioate of the formula 8. Compound according to claim 1 wherein such compound is O (2-nitro-4-n-propoXy-pheny1)-O-methyl-N- isopropyl-phosphoro-amido-thioate of the formula i-CaHrNH 9. Compound according to claim 1 wherein such compound is 0 (2 nitro 4-ethoxy-phenyl)-O-ethyl-N-isopropyl-phosphoro-amido-thioate of the formula 10. Compound according to claim 1 wherein such compound is O-(2-nitro-4-methoxy-phenyl)-O-n-butyl-N-isopropyl-phosphoro-amido-thioate of the formula l.- CaHz-NH References Cited UNITED STATES PATENTS 2,875,233 2/1959 Blair et al 260-951 R 3,472,920 10/1969 Schrader et al. 260-954 3,322,864 5/1967 Schrader 260-954 3,444,274 5/1969 Schrader 260-954 LEWIS GO'ITS, Primary Examiner R. L. RAYMOND, Assistant Examiner US. Cl. X.R. 

